Colon Cancer: Gene >> TRAF6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000348124
Start	36489986:36489986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1421T>C
AA Mutation	p.Val474Ala(p.V474A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000348124
Start	36501260:36501260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.256G>A
AA Mutation	p.Gly86Ser(p.G86S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000348124
Start	36497257:36497257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.457G>T
AA Mutation	p.Ala153Ser(p.A153S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000348124
Start	36490403:36490403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1004G>A
AA Mutation	p.Arg335Gln(p.R335Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000348124
Start	36490068:36490068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1339G>A
AA Mutation	p.Glu447Lys(p.E447K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348124
Start	36498538:36498538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.399A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348124
Start	36490213:36490213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751475632
CDS Mutation	c.1194G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000348124
Start	36490404:36490404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1003C>T
AA Mutation	p.Arg335Ter(p.R335*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TRAF6

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348124
Start	36489949:36489949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1458T>C
Mutation Classification	Silent
Feature Type	Transcript